NDC 71610-582

Bupropion Hydrochloride SR 200 mg tablet, film coated, extended release

On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. rebottles it from Radha Pharmaceuticals, Inc.'s NDC 77771-176.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it and tests it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Bupropion: every company that makes it
Form
tablet, film coated, extended release, oral
Strength
200 mg
Approval
ANDA ANDA205794
On the market since
Apr 15, 2021
Package NDCs
71610-582-42 71610-582-83
Official label
DailyMed (National Library of Medicine), updated Sep 29, 2026

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